Canonical Allele Identifier: CA346502084
Gene: SPAST HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.32136612A>C , CM000664.2:g.32136612A>C GRCh38
NC_000002.11:g.32361681A>C , CM000664.1:g.32361681A>C GRCh37
NC_000002.10:g.32215185A>C NCBI36
NG_008730.1:g.78002A>C , LRG_714:g.78002A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000704289.1:c.*955A>C ENSP00000515816.1:n.*955A>C
ENST00000315285.9:c.1295A>C MANE Select ENSP00000320885.3:p.Glu432Ala
ENST00000621856.2:c.1292A>C ENSP00000482496.2:p.Glu431Ala
ENST00000642281.1:c.1032A>C
ENST00000642455.1:c.1196A>C ENSP00000493827.1:p.Glu399Ala
ENST00000642751.1:c.1069A>C
ENST00000642999.1:c.1037A>C ENSP00000496589.1:p.Glu346Ala
ENST00000643327.1:c.454A>C
ENST00000643334.1:c.875A>C
ENST00000644408.1:c.1171A>C
ENST00000644954.1:c.941A>C ENSP00000494312.1:p.Glu314Ala
ENST00000645159.1:n.2032A>C
ENST00000645671.1:c.745A>C
ENST00000645730.1:c.593-497A>C
ENST00000646082.1:c.941A>C
ENST00000646571.1:c.1199A>C ENSP00000495015.1:p.Glu400Ala
ENST00000647007.1:n.987A>C
ENST00000647133.1:c.795A>C
ENST00000315285.7:c.1295A>C ENSP00000320885.3:p.Glu432Ala
ENST00000345662.5:c.1199A>C ENSP00000340817.1:p.Glu400Ala
ENST00000615843.4:c.1295A>C ENSP00000480893.1:p.Glu432Ala
ENST00000621856.1:c.1037A>C ENSP00000482496.1:p.Glu346Ala
NM_014946.3:c.1295A>C , LRG_714t1:c.1295A>C NP_055761.2:p.Glu432Ala
NM_199436.1:c.1199A>C NP_955468.1:p.Glu400Ala
XM_005264516.3:c.1292A>C XP_005264573.1:p.Glu431Ala
XM_011533067.1:c.1295A>C XP_011531369.1:p.Glu432Ala
NM_001363823.1:c.1292A>C NP_001350752.1:p.Glu431Ala
NM_001363875.1:c.1196A>C NP_001350804.1:p.Glu399Ala
XM_005264516.5:c.1292A>C XP_005264573.1:p.Glu431Ala
XM_011533067.2:c.1295A>C XP_011531369.1:p.Glu432Ala
XM_017004778.2:c.1199A>C XP_016860267.1:p.Glu400Ala
NM_001363823.2:c.1292A>C NP_001350752.1:p.Glu431Ala
NM_001363875.2:c.1196A>C NP_001350804.1:p.Glu399Ala
NM_001377959.1:c.1199A>C NP_001364888.1:p.Glu400Ala
NM_014946.4:c.1295A>C MANE Select NP_055761.2:p.Glu432Ala
NM_199436.2:c.1199A>C NP_955468.1:p.Glu400Ala